"Kawasumi" hemodialyzer
- Analysis ID
- 14d3ff7815d167af8643218f2493cd55
- Customs Code
- DHA00601701807
- Manufacturer
- KAWASUMI LABORATORIES,INC. MIE FACTORY
- Manufacturer Country
- Japan
- Authorized Representative
- Taiwan Asahi Kasei Medical Device Trading Co., Ltd
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- H Gastroenterology and urology
- Product Type (Level 2)
- H.5860 高滲透性之血液透析系統
- Import Information
- import
- Registration Date
- Aug 18, 2006
- Expiry Date
- Aug 18, 2011
- Cancellation Date
- Jan 14, 2013
- Status
- Logged out
- Reason
- 許可證已逾有效期
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Access comprehensive regulatory information for "Kawasumi" hemodialyzer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 14d3ff7815d167af8643218f2493cd55 and manufactured by KAWASUMI LABORATORIES,INC. MIE FACTORY. The authorized representative in Taiwan is Taiwan Asahi Kasei Medical Device Trading Co., Ltd.
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including KAWASUMI LABORATORIES INC. MIE FACTORY, and 1 recent registrations in the same category. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.